Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

G/C | Ancestral: C | Ambiguity code: S | MAF: 0.22 (C)

Chromosome 16:50769845 (forward strand) | View in location tab

Most severe consequence
Evidence status


This variation has 12 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_ImmunoChip, Affy GenomeWideSNP_6.0

About this variant

This variant overlaps 10 transcripts, has 2567 individual genotypes and is mentioned in 1 citation.

Variation displays